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EXPERIMENTAL AND QUANTUM-CHEMICAL STUDY OF THE REACTIONS OF 1,10-ANTHRAQUINONES WITH ALCOHOLS AND AMINES Full article

Journal Tetrahedron
ISSN: 0040-4020
Output data Year: 1995, Volume: 51, Number: 10, Pages: 3061-3076 Pages count : 16 DOI: 10.1016/0040-4020(95)00046-B
Authors Gritsan N.P. 1 , Klimenko L.S. 2 , Leonenko Z.V. 1 , Mainagashev I.Ya. 2 , Mamatyuk V.I. 2 , Vetchinov V.P. 2
Affiliations
1 Institute of Chemical Kinetics and Combustion and Novosibirsk State University, 630090, Novosibirsk, Russia
2 Institute of Organic Chemistry, 630090, Novosibirsk, Russia

Abstract: The primary stage of the reaction between 9-aryloxy-1,10-anthraquinones and methanol is the nucleophilic 1,4-addition which gives rise to the adduct, corresponding to 1-hydroxy-9-methoxy-9-aryloxy-10-anthrone. The reaction of 9-aryloxy-1,10-anthraquinones with the primary aliphatic and aromatic amines results in the formation of 9-alkyl(aryl)aminol-1,10-anthraquinones that are in a tautomeric equilibrium with 1-hydroxy-9,10-anthraquinone-9-alkyl(aryl)imines. The quantum chemical calculations of the enthalpy of 9-amine-1,10-anthraquinone isomerization are in agreement with the experimentally recorded influence on the tautomeric equilibrium of the nature of amine, solvent, and substituent in the anthraquinone nucleus. The data of quantum chemical calculations confirm the addition-elimination mechanism of the reaction of 1,10-anthraquinones with amines.
Cite: Gritsan N.P. , Klimenko L.S. , Leonenko Z.V. , Mainagashev I.Y. , Mamatyuk V.I. , Vetchinov V.P.
EXPERIMENTAL AND QUANTUM-CHEMICAL STUDY OF THE REACTIONS OF 1,10-ANTHRAQUINONES WITH ALCOHOLS AND AMINES
Tetrahedron. 1995. V.51. N10. P.3061-3076. DOI: 10.1016/0040-4020(95)00046-B WOS Scopus OpenAlex
Dates:
Published print: Mar 1, 1995
Identifiers:
Web of science: WOS:A1995QL65700020
Scopus: 2-s2.0-0028815511
OpenAlex: W2013068984
Citing:
DB Citing
Web of science 18
Scopus 19
OpenAlex 19
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